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Journal Abstract Search

448 related items for PubMed ID: 17435464

  • 21. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
    Varela MC, Lopes GM, Koiffmann CP.
    Ann Genet; 2004; 47(3):267-73. PubMed ID: 15337472
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  • 22. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.
    Lukusa T, Fryns JP.
    Genet Couns; 2000; 11(2):119-26. PubMed ID: 10893663
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  • 23. Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
    Giurgiutiu DV, Espinoza LM, Wood TC, DuPont BR, Holden KR.
    J Child Neurol; 2008 Jan; 23(1):112-7. PubMed ID: 18184946
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  • 24. Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome.
    Koukoui SD, Chaudhuri A.
    Brain Res Rev; 2007 Jan; 53(1):27-38. PubMed ID: 16844227
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  • 25. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome].
    Witkowski R, Ullrich E, Pietsch P, Weber K, Heller K, Losanowa T, Nitz I.
    Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109
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  • 26. The behavioral phenotype of FMR1 mutations.
    Boyle L, Kaufmann WE.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):469-76. PubMed ID: 20981777
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  • 32. Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings.
    Dimitropoulos A, Schultz RT.
    Curr Psychiatry Rep; 2007 Apr 15; 9(2):159-64. PubMed ID: 17389128
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  • 34. Dorsal and ventral stream mediated visual processing in genetic subtypes of Prader-Willi syndrome.
    Woodcock KA, Humphreys GW, Oliver C.
    Neuropsychologia; 2009 Oct 15; 47(12):2367-73. PubMed ID: 18950649
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  • 36. Genes for Prader Willi syndrome/Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression.
    Fischer KM.
    Med Hypotheses; 1996 Oct 15; 47(4):289-98. PubMed ID: 8910878
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  • 40. Metformin as targeted treatment in fragile X syndrome.
    Dy ABC, Tassone F, Eldeeb M, Salcedo-Arellano MJ, Tartaglia N, Hagerman R.
    Clin Genet; 2018 Feb 15; 93(2):216-222. PubMed ID: 28436599
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